ENST00000358602.9:c.7752+138T>C
MANE Select
|
ENSP00000351416.4:n.7752+138T>C
|
|
ENST00000330838.10:c.6999+138T>C
|
ENSP00000332265.6:n.6999+138T>C
|
|
ENST00000358602.8:c.7752+138T>C
|
ENSP00000351416.4:n.7752+138T>C
|
|
ENST00000509867.6:c.7413+138T>C
|
ENSP00000427151.2:n.7413+138T>C
|
|
ENST00000558247.5:c.7403+138T>C
|
|
|
NM_001286771.1:c.7413+138T>C
|
NP_001273700.1:n.7413+138T>C
|
|
NM_032217.3:c.7752+138T>C
|
NP_115593.3:n.7752+138T>C
|
|
NM_198889.1:c.6999+138T>C
|
NP_942592.1:n.6999+138T>C
|
|
XM_005265667.3:c.7749+138T>C
|
XP_005265724.1:n.7749+138T>C
|
|
XM_005265671.3:c.6996+138T>C
|
XP_005265728.1:n.6996+138T>C
|
|
NM_001286771.2:c.7413+138T>C
|
NP_001273700.1:n.7413+138T>C
|
|
NM_015574.1:c.7749+138T>C
|
NP_056389.1:n.7749+138T>C
|
|
NM_032217.4:c.7752+138T>C
|
NP_115593.3:n.7752+138T>C
|
|
NM_198889.2:c.6999+138T>C
|
NP_942592.1:n.6999+138T>C
|
|
XM_005265671.4:c.6996+138T>C
|
XP_005265728.1:n.6996+138T>C
|
|
XM_017008011.1:c.7410+138T>C
|
XP_016863500.1:n.7410+138T>C
|
|
XM_017008012.1:c.6660+138T>C
|
XP_016863501.1:n.6660+138T>C
|
|
XM_017008013.1:c.6657+138T>C
|
XP_016863502.1:n.6657+138T>C
|
|
NM_001286771.3:c.7413+138T>C
|
NP_001273700.1:n.7413+138T>C
|
|
NM_015574.2:c.7749+138T>C
|
NP_056389.1:n.7749+138T>C
|
|
NM_032217.5:c.7752+138T>C
MANE Select
|
NP_115593.3:n.7752+138T>C
|
|
NM_198889.3:c.6999+138T>C
|
NP_942592.1:n.6999+138T>C
|
|